An investigation of the mechanism of activation of tryptophan by tryptophanyl-tRNA synthetase from beef pancreas.

Adenosine (S)-5'-[alpha-17O, 18O2]triphosphate has been synthesized and used to investigate the stereochemical course of activation of tryptophan by tryptophanyl-tRNA synthetase from beef pancreas. It is shown that the reaction proceeds by displacement of Mg pyrophosphate from MgATP with inversion of configuration at P alpha. Tryptophanyl-tRNA synthetase catalyses positional isotope exchange in adenosine 5'-[beta-18O2]triphosphate in the presence of tryptophan but not in its absence or in the presence of the competitive inhibitors tryptamine and tryptophanol. These observations eliminate a multi-adenylyl transfer or dissociative mechanism and in combination with the sterochemical study leave a direct associative 'in line' displacement at P alpha of MgATP as the only tenable mechanism for the activation of tryptophan by tryptophanyl-tRNA synthetase.